A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620956



Internal ID7007826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86383916..86386335hg38UCSC Ensembl
Innerchr9:86383927..86386324hg38UCSC Ensembl
Outerchr9:86383905..86386346hg38UCSC Ensembl
chr9:88998831..89001250hg19UCSC Ensembl
Innerchr9:88998842..89001239hg19UCSC Ensembl
Outerchr9:88998820..89001261hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382420
hg192420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13544305
SamplesHG02095
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620956
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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